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Peer Review reports

From: An FGFR2 mutation as the potential cause of a new phenotype including early-onset osteoporosis and bone fractures: a case report

Original Submission
26 Jun 2023 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
11 Aug 2023 Reviewed Reviewer Report
17 Aug 2023 Reviewed Reviewer Report
7 Sep 2023 Author responded Author comments - Mariia Parfenenko
Resubmission - Version 4
7 Sep 2023 Submitted Manuscript version 4
28 Sep 2023 Author responded Author comments - Mariia Parfenenko
Resubmission - Version 5
28 Sep 2023 Submitted Manuscript version 5
28 Sep 2023 Author responded Author comments - Mariia Parfenenko
Resubmission - Version 6
28 Sep 2023 Submitted Manuscript version 6
12 Oct 2023 Author responded Author comments - Mariia Parfenenko
Resubmission - Version 7
12 Oct 2023 Submitted Manuscript version 7
17 Oct 2023 Author responded Author comments - Mariia Parfenenko
Resubmission - Version 8
17 Oct 2023 Submitted Manuscript version 8
31 Oct 2023 Reviewed Reviewer Report
5 Nov 2023 Reviewed Reviewer Report
20 Nov 2023 Author responded Author comments - Mariia Parfenenko
Resubmission - Version 9
20 Nov 2023 Submitted Manuscript version 9
Publishing
22 Nov 2023 Editorially accepted
14 Dec 2023 Article published 10.1186/s12920-023-01750-1

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